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Test ID BLOD1317 MI-2

Reporting Name

MI-2

Performing Laboratory

RDL Reference Laboratory, Inc.

Specimen Type

Varies


Specimen Required


Submit only 1 of the following

 

Serum

Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 1 mL of serum refrigerate in plastic vial.

 

Plasma

Draw blood in a lavender-top (EDTA) tube(s). Spin down and send 1 mL of EDTA plasma refrigerate in plastic vial.


Specimen Minimum Volume

1 mL

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated (preferred) 7 days
  Frozen  180 days
  Ambient  7 days

Reference Values

Negative

 

Day(s) and Time(s) Performed

Monday through Friday

Test Classification

This test was developed and its performance characteristics validated by RDL. There is no FDA approved assay for this test. As a lab developed test (LDT), approval or clearance by the FDA is not required. This test may be used for clinical purposes and should not be regarded as investigational or for research.

CPT Code Information

83516

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FMI2 MI-2 In Process

 

Result ID Test Result Name Result LOINC Value
Z2421 MI-2 18485-3

Reject Due To

Hemolysis:

Mild OK ; Gross Reject

Thawing:

Warm OK; Cold OK

Lipemia:

Mild OK ; Gross Reject

Icteric:

Mild OK ; Gross Reject

Other:

NA

Method Name

Immunoprecipitation (IPP)